Canonical Allele Identifier: CA1594081677
Gene: ITK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.157241366_157241368delinsAAT , CM000667.2:g.157241366_157241368delinsAAT GRCh38
NC_000005.9:g.156668376_156668378delinsAAT , CM000667.1:g.156668376_156668378delinsAAT GRCh37
NC_000005.8:g.156600954_156600956delinsAAT NCBI36
NG_016276.1:g.65470_65472delinsAAT , LRG_189:g.65470_65472delinsAAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000696962.1:c.852-280_852-278delinsAAT ENSP00000513001.1:n.852-280_852-278delinsAAT
ENST00000422843.8:c.986-280_986-278delinsAAT MANE Select ENSP00000398655.4:n.986-280_986-278delinsAAT
ENST00000422843.7:c.986-280_986-278delinsAAT ENSP00000398655.3:n.986-280_986-278delinsAAT
ENST00000519402.5:n.2291_2293delinsAAT
ENST00000520173.1:n.104-280_104-278delinsAAT
NM_005546.3:c.986-280_986-278delinsAAT , LRG_189t1:c.986-280_986-278delinsAAT NP_005537.3:n.986-280_986-278delinsAAT
XM_017009443.1:c.611-280_611-278delinsAAT XP_016864932.1:n.611-280_611-278delinsAAT
NM_005546.4:c.986-280_986-278delinsAAT MANE Select NP_005537.3:n.986-280_986-278delinsAAT